Contribution of gastric oxidation to ethanol first-pass metabolism in baboons

Citation
E. Baraona et al., Contribution of gastric oxidation to ethanol first-pass metabolism in baboons, ALC CLIN EX, 24(7), 2000, pp. 946-951
Citations number
40
Categorie Soggetti
Clinical Psycology & Psychiatry","Neurosciences & Behavoir
Journal title
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
ISSN journal
01456008 → ACNP
Volume
24
Issue
7
Year of publication
2000
Pages
946 - 951
Database
ISI
SICI code
0145-6008(200007)24:7<946:COGOTE>2.0.ZU;2-3
Abstract
Background: A portion of ingested alcohol does not reach the systemic blood , undergoing a first-pass metabolism (FPM) during gastric and hepatic circu lation. Methods: To determine whether the stomach can metabolize sufficient ethanol to account for the FPM, and to what extent gastric alcohol dehydrogenase ( ADH) activity is responsible, the hepatic vein, the portal vein. and the ao rta were cannulated nonocclusively in baboons to measure the conversion of ethanol to acetate in vivo. C-14-ethanol (300 mg/kg as a 15% solution) was given intragastrically (IG) whereas H-3-acetate was continuously infused in travenously (IV).C-14-acetate was measured after exhaustive evaporation of ethanol. Simultaneous sampling of hepatic venous, portal and arterial blood was carried out for 3 hr, at the end of which the same alcohol dose was gi ven IV to calculate the Michaelis-Menten parameters of elimination. Results: Analysis of the IV and IG ethanol curves revealed a FPM of 94 +/- 11 mg/kg (31% of dose). The portal-arterial differences were negative for H -3-acetate (indicating net extraction) and positive for C-14-ethanol and C- 14-acetate (indicating net output). Portal acetate production (extraction p lus net output multiplied by the portal plasma flow) increased with time an d accounted, over the first 3 hr (82 +/- 13 mg/kg), for 87% of the FPM. Alc ohol oxidation by gastric ADH activity (28.7 +/- 7.2 mg/kg) accounted for o nly 31% of the FPM. Conclusions: The in vivo oxidation of ethanol to acetate in the upper diges tive tract accounts for the FPM of ethanol and is mediated, at least in par t, by ADH activity.